Number of the records: 1
Laurenceov-Moonov syndróm
SYS d007849 LBL 00000nz--a2200000o--4500 005 20260512091035.0 008 990101|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a C10.228.140.617.500 065 $a C16.131.077.509 066 $a 01 $c 03 150 $a Laurenceov-Moonov syndróm $x BL $x CF $x CI $x CL $x CO $x DG $x DH $x DI $x DT $x EC $x EH $x EM $x EN $x EP $x ET $x GE $x HI $x IM $x ME $x MI $x MO $x NU $x PA $x PC $x PP $x PS $x PX $x RH $x RT $x SU $x TH $x UR $x VE $x VI $2 slo 450 $w v $a Laurence-Moon-Biedl Syndrome $2 eng 450 $w v $a Laurenceov-Moonov-Biedlov syndróm $2 slo 450 $w v $a degenerácia diencefaloretinálna $2 slo 550 $7 sllk_us_auth*d008607 $Y Intellectual Disability $w p $a postihnutie intelektuálne 665 $a 2000 (1966) $2 eng 680 $a note entry term: do not confuse with LAURENCE-MOON-BARDET-BIEDL SYNDROME see BARDET-BIEDL SYNDROME $2 eng 680 9-
$i An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY. This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity. (From N Engl J Med. 1989 Oct 12;321(15):1002-9) $2 eng 750 -2
$a Laurence-Moon Syndrome $2 eng 980 $x M
Number of the records: 1